rs11552822
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs11552822(G;T) |
| Make rs11552822(T;T) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 9 |
| Position | 21971109 |
| Gene | CDKN2A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11552822 |
| dbSNP (classic) | rs11552822 |
| ClinGen | rs11552822 |
| ebi | rs11552822 |
| HLI | rs11552822 |
| Exac | rs11552822 |
| Gnomad | rs11552822 |
| Varsome | rs11552822 |
| LitVar | rs11552822 |
| Map | rs11552822 |
| PheGenI | rs11552822 |
| Biobank | rs11552822 |
| 1000 genomes | rs11552822 |
| hgdp | rs11552822 |
| ensembl | rs11552822 |
| geneview | rs11552822 |
| scholar | rs11552822 |
| rs11552822 | |
| pharmgkb | rs11552822 |
| gwascentral | rs11552822 |
| openSNP | rs11552822 |
| 23andMe | rs11552822 |
| SNPshot | rs11552822 |
| SNPdbe | rs11552822 |
| MSV3d | rs11552822 |
| GWAS Ctlg | rs11552822 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs11552822(A;A) rs11552822(T;T) |
| Alt | rs11552822(A;A) rs11552822(T;T) |
| Reference | Rs11552822(G;G) |
| Significance | Probable-Pathogenic |
| Disease | Neoplasm Hereditary cancer-predisposing syndrome Hereditary cutaneous melanoma |
| Variation | info |
| Gene | CDKN2A |
| CLNDBN | Neoplasm Hereditary cancer-predisposing syndrome Hereditary cutaneous melanoma |
| Reversed | 1 |
| HGVS | NC_000009.11:g.21971108C>A; NC_000009.11:g.21971108C>T |
| CLNSRC | |
| CLNACC | RCV000419046.1, RCV000214736.1, RCV000474240.1, |
